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Titan Spine, Inc.

5 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic Interbody Fusion Device (K191581)Titan Spine, Inc.2020-01-08
Endoskeleton TAS Plate (K192054)Titan Spine, Inc.2019-08-29
Endoskeleton TA Interbody Fusion Device, Endoskeleton TAS and TAS Hyperlordotic Interbody Fusion Device, Endoskeleton TO Interbody Fusion Device, Endoskeleton TT Interbody Fusion Device, Endoskeleton TC Interbody Fusion Device, Endoskeleton TCS Interbody Fusion Device, Endoskeleton TL Interbody Fusion Device (K192018)Titan Spine, Inc.2019-08-16
Endoskeleton TCS Interbody Fusion Device (K191565)Titan Spine, Inc.2019-08-06
Endoskeleton® TA Interbody Fusion Device, Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TO Interbody Fusion Device, Endoskeleton® TT Interbody Fusion Device, Endoskeleton® TC Interbody Fusion Device, Endoskeleton® TCS Interbody Fusion Device, Endoskeleton® TL Interbody Fusion Device, Endoskeleton® TA Vertebral Body Replacement (VBR) Device (K183557)Titan Spine, Inc.2019-02-11

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Every clearance here is in the API, with alerts when new ones post.